FdaApplication
ANDA 201833
Identifiers
- fda_app_no: ANDA201833
Properties
| Property | Value |
|---|---|
| applicant_name | HIKMA PHARMS |
| application_type | ANDA |
| approval_date | 2013-09-24 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| SODIUM CHLORIDE 0.9% | SODIUM CHLORIDE | 90MG/10ML (9MG/ML) | SOLUTION;INJECTION |
| SODIUM CHLORIDE 0.9% | SODIUM CHLORIDE | 18MG/2ML (9MG/ML) | SOLUTION;INJECTION |
2 products